A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580081



Internal ID16367490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53369175..53426434hg38UCSC Ensembl
Innerchr19:53872428..53929687hg19UCSC Ensembl
Innerchr19:58564240..58621499hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3857260
hg1957260
hg1857260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6535n54
Supporting Variantsnssv901160
Samples
Known GenesZNF525, ZNF765
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580081
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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